A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267348



Internal ID20476566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86298252..86298252hg38UCSC Ensembl
chr15:86841483..86841483hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756918
Supporting Variants
Samples
Known GenesAGBL1, AGBL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267348
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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